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Microlife OXY550 BT

by Microlife USA, Inc.

Microlife OXY550 BT is a Class II device made by Microlife USA, Inc., listed in FDA GUDID since 21 Nov 2022 (UDI-DI 00642632950249), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00642632950249 UDI-DI Date21 Nov 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Microlife
Generic name
Pulse oximeter
Model / reference
OXY550 BT
Primary DI / UDI-DI
00642632950249
FDA product code
DQA
GMDN term
Pulse oximeter
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pulse oximeter

Other devices from Microlife USA, Inc.

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Properties

  • Lot / batch number
Other properties (14, all answered No)